Canonical Allele Identifier: PA295772
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 137839
ClinVar RCV Id: RCV000154988 RCV000266819 RCV000303282 RCV000306728 RCV000263263 RCV000357808 RCV000472153 RCV000769066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile5077Val
CA295771
NM_133378.4:c.15229A>G